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Laura Lucarini

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L Evangelisti; Laura Lucarini; M Attanasio; Ilaria Lapini; Betti Giusti; C Porciani; Gianfranco Gensini; Rosanna Abbate; Guglielmina Pepe
A single heterozygous nucleotide substitution displays two different altered mechanisms in the FBN1 gene of five Italian Marfan patients.
Lucia Evangelisti; Monica Attanasio; Laura Lucarini; Francesco Sofi; Rossella Marcucci; Cristina Giglioli; Serafina Valente; Gf Gensini; Rosanna Abbate; Guglielmina Pepe
PPARgamma promoter polymorphisms and acute coronary syndrome.
Laura Lucarini; Elena Sticchi; Francesco Sofi; Giovanni Pratesi; Carlo Pratesi; Raffaele Pulli; Gian Franco Gensini; Rosanna Abbate; Guglielmina Pepe; Cinzia Fatini
ACE and TGFBR1 genes interact in influencing the susceptibility to abdominal aortic aneurysm.

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All Publications

2010: L Evangelisti; Laura Lucarini; M Attanasio; Ilaria Lapini; Betti Giusti; C Porciani; Gianfranco Gensini; Rosanna Abbate; Guglielmina Pepe
A single heterozygous nucleotide substitution displays two different altered mechanisms in the FBN1 gene of five Italian Marfan patients.
European journal of medical genetics 2010;53(5):299-302.
2009: Lucia Evangelisti; Monica Attanasio; Laura Lucarini; Francesco Sofi; Rossella Marcucci; Cristina Giglioli; Serafina Valente; Gf Gensini; Rosanna Abbate; Guglielmina Pepe
PPARgamma promoter polymorphisms and acute coronary syndrome.
Atherosclerosis 2009;205(1):186-91.
2009: Laura Lucarini; Elena Sticchi; Francesco Sofi; Giovanni Pratesi; Carlo Pratesi; Raffaele Pulli; Gian Franco Gensini; Rosanna Abbate; Guglielmina Pepe; Cinzia Fatini
ACE and TGFBR1 genes interact in influencing the susceptibility to abdominal aortic aneurysm.
Atherosclerosis 2009;202(1):205-10.
2008: Monica Monici; Venere Basile; Giovanni Romano; Lucia Evangelisti; Laura Lucarini; Monica Attanasio; Enrico Bertini; Franco Fusi; Gian Franco Gensini; Guglielmina Pepe
Fibroblast autofluorescence in connective tissue disorders: a future tool for clinical and differential diagnosis?
Journal of biomedical optics 2008;13(5):054025.
2008: Monica Attanasio; Ilaria Lapini; Lucia Evangelisti; Laura Lucarini; Betti Giusti; Maria Cristina Porciani; R Fattori; Chiara Anichini; Rosanna Abbate; Gf Gensini; Guglielmina Pepe
FBN1 mutation screening of patients with Marfan syndrome and related disorders: detection of 46 novel FBN1 mutations.
Clinical genetics 2008;74(1):39-46.
2007: Stefania Petrini; Adele D'Amico; sale Patrizio; Laura Lucarini; Patrizia Sabatelli; Alessandra Tessa; Betti Giusti; Margherita Verardo; Rosalba Carrozzo; Elisabetta Mattioli; Marina Scarpelli; Mon-Li Chu; Guglielmina Pepe; Matteo A Russo; Enrico Bertini
Ullrich myopathy phenotype with secondary ColVI defect identified by confocal imaging and electron microscopy analysis.
Neuromuscular disorders : NMD 2007;17(8):587-96.
2007: Guglielmina Pepe; Ilaria Lapini; Lucia Evangelisti; Monica Attanasio; Betti Giusti; Laura Lucarini; Rossella Fattori; Giannantonio Pellicanò; Mario Scrivanti; Maria Cristina Porciani; Rosanna Abbate; Andrea Alberto Conti
Is ectopia lentis in some cases a mild phenotypic expression of Marfan syndrome? Need for a long-term follow-up.
Molecular vision 2007;13():2242-7.
2006: Guglielmina Pepe; Laura Lucarini; Rui-Zhu Zhang; Te-Cheng Pan; Betti Giusti; Susana Quijano-Roy; Corine Gartioux; K M D Bushby; Pascale Guicheney; Mon-Li Chu
COL6A1 genomic deletions in Bethlem myopathy and Ullrich muscular dystrophy.
Annals of neurology 2006;59(1):190-5.
2005: Betti Giusti; Laura Lucarini; Valentina Pietroni; Simona Lucioli; Brunella Bandinelli; Patrizia Sabatelli; Stefano Squarzoni; Stefania Petrini; Corine Gartioux; Beril Talim; Filip Roelens; Luciano Merlini; Haluk Topaloglu; Enrico Bertini; Pascale Guicheney; Guglielmina Pepe
Dominant and recessive COL6A1 mutations in Ullrich scleroatonic muscular dystrophy.
Annals of neurology 2005;58(3):400-10.
2005: Laura Lucarini; Betti Giusti; Rui-Zhu Zhang; Te-Cheng Pan; Cecilia Jimenez-Mallebrera; Eugenio Mercuri; Francesco Muntoni; Guglielmina Pepe; Mon-Li Chu
A homozygous COL6A2 intron mutation causes in-frame triple-helical deletion and nonsense-mediated mRNA decay in a patient with Ullrich congenital muscular dystrophy.
Human genetics 2005;117(5):460-6.
2005: Simona Lucioli; Betti Giusti; Eugenio Mercuri; Olga Camacho Vanegas; Laura Lucarini; V Pietroni; Andoni Urtizberea; Rabah Ben Yaou; Marianne De Visser; Anneke J van der Kooi; CG Bönnemann; S T Iannaccone; Luciano Merlini; Kate Bushby; Francesco Muntoni; Enrico Bertini; Mon-Li Chu; Guglielmina Pepe
Detection of common and private mutations in the COL6A1 gene of patients with Bethlem myopathy.
Neurology 2005;64(11):1931-7.
2004: Anna Maria Gori; Monica Attanasio; Alessandra Gazzini; L Rossi; Laura Lucarini; S Miletti; J Chini; Marco Manoni; Rosanna Abbate; Andrea Alberto Conti
Cytokine gene expression and production by human LPS-stimulated mononuclear cells are inhibited by sulfated heparin-like semi-synthetic derivatives.
Journal of thrombosis and haemostasis : JTH 2004;2(9):1657-62.
1999: Letzia Giurlani; Guglielmina Pepe; Betti Giusti; Monica Attanasio; P Comeglio; Maria Cristina Porciani; Lucia Evangelisti; Tamara Brunelli; Laura Lucarini; Rosanna Abbate
[Marfan's syndrome. Clinical and molecular characterization of 51 Italian patients].
Minerva cardioangiologica 1999;47(12):544.